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1. (WO1998050364) TETRAHYDROISOQUINOLINE DERIVATIVES AS MODULATORS OF DOPAMINE D¿3? RECEPTORS
Latest bibliographic data on file with the International Bureau   

Pub. No.: WO/1998/050364 International Application No.: PCT/EP1998/002583
Publication Date: 12.11.1998 International Filing Date: 27.04.1998
Chapter 2 Demand Filed: 07.11.1998
IPC:
C07D 217/04 (2006.01) ,C07D 217/26 (2006.01) ,C07D 401/12 (2006.01) ,C07D 405/12 (2006.01) ,C07D 409/12 (2006.01) ,C07D 413/12 (2006.01) ,C07D 471/04 (2006.01) ,C07D 487/04 (2006.01) ,C07D 495/04 (2006.01)
C CHEMISTRY; METALLURGY
07
ORGANIC CHEMISTRY
D
HETEROCYCLIC COMPOUNDS
217
Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems
02
with only hydrogen atoms or radicals containing only carbon and hydrogen atoms, directly attached to carbon atoms of the nitrogen-containing ring; Alkylene-bis-isoquinolines
04
with hydrocarbon or substituted hydrocarbon radicals attached to the ring nitrogen atom
C CHEMISTRY; METALLURGY
07
ORGANIC CHEMISTRY
D
HETEROCYCLIC COMPOUNDS
217
Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems
22
with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to carbon atoms of the nitrogen-containing ring
26
Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
C CHEMISTRY; METALLURGY
07
ORGANIC CHEMISTRY
D
HETEROCYCLIC COMPOUNDS
401
Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
02
containing two hetero rings
12
linked by a chain containing hetero atoms as chain links
C CHEMISTRY; METALLURGY
07
ORGANIC CHEMISTRY
D
HETEROCYCLIC COMPOUNDS
405
Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
02
containing two hetero rings
12
linked by a chain containing hetero atoms as chain links
C CHEMISTRY; METALLURGY
07
ORGANIC CHEMISTRY
D
HETEROCYCLIC COMPOUNDS
409
Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
02
containing two hetero rings
12
linked by a chain containing hetero atoms as chain links
C CHEMISTRY; METALLURGY
07
ORGANIC CHEMISTRY
D
HETEROCYCLIC COMPOUNDS
413
Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
02
containing two hetero rings
12
linked by a chain containing hetero atoms as chain links
C CHEMISTRY; METALLURGY
07
ORGANIC CHEMISTRY
D
HETEROCYCLIC COMPOUNDS
471
Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/-C07D463/251
02
in which the condensed system contains two hetero rings
04
Ortho-condensed systems
C CHEMISTRY; METALLURGY
07
ORGANIC CHEMISTRY
D
HETEROCYCLIC COMPOUNDS
487
Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/-C07D477/183
02
in which the condensed system contains two hetero rings
04
Ortho-condensed systems
C CHEMISTRY; METALLURGY
07
ORGANIC CHEMISTRY
D
HETEROCYCLIC COMPOUNDS
495
Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
02
in which the condensed system contains two hetero rings
04
Ortho-condensed systems
Applicants:
BRANCH, Clive, Leslie [GB/GB]; GB (UsOnly)
JOHNSON, Christopher, Norbert [GB/GB]; GB (UsOnly)
STEMP, Geoffrey [GB/GB]; GB (UsOnly)
SMITHKLINE BEECHAM PLC [GB/GB]; New Horizons Court Brentford Middlesex TW8 9EP, GB (AL, AM, AT, AU, AZ, BA, BB, BE, BF, BG, BJ, BR, BY, CA, CF, CG, CH, CI, CM, CN, CU, CY, CZ, DE, DK, EE, ES, FI, FR, GA, GB, GE, GH, GM, GN, GR, GW, HU, ID, IE, IL, IS, IT, JP, KE, KG, KP, KR, KZ, LC, LK, LR, LS, LT, LU, LV, MC, MD, MG, MK, ML, MN, MR, MW, MX, NE, NL, NO, NZ, PL, PT, RO, RU, SD, SE, SG, SI, SK, SL, SN, SZ, TD, TG, TJ, TM, TR, TT, UA, UG, UZ, VN, YU, ZW)
Inventors:
BRANCH, Clive, Leslie; GB
JOHNSON, Christopher, Norbert; GB
STEMP, Geoffrey; GB
Agent:
GARRETT, Michael; SmithKline Beecham plc Corporate Intellectual Property Two New Horizons Court Brentford Middlesex TW8 9EP, GB
GIDDINGS, Peter, John; SmithKline_Beecham p.l.c. Corporate Intellectual Property Two New Horizons Court Brentford Middlesex TW8 9EP, GB
Priority Data:
9708976.703.05.1997GB
9723294.604.11.1997GB
Title (EN) TETRAHYDROISOQUINOLINE DERIVATIVES AS MODULATORS OF DOPAMINE D3 RECEPTORS
(FR) DERIVES DE TETRAHYDROISOQUINOLINE COMME MODULATEURS DES RECEPTEURS D3 DE LA DOPAMINE
Abstract:
(EN) Compounds of formula (I) wherein: R represents a substituent selected from: a hydrogen or a substituent as defined in the claims; R2 represents a hydrogen atom or a C1-4alkyl group; q is 1 or 2; A represents a group of formula (a), (b) or (c) wherein: Ar represents an optionally substituted phenyl ring or an optionally substituted 5- or 6-membered aromatic heterocyclic ring; or an optionally substituted bicyclic ring system; Ar1 and Ar2 each independently represent an optionally substituted phenyl ring or an optionally substituted 5- or 6-membered aromatic heterocyclic ring; and Y represents a bond, -NHCO-, -CONH-, -CH2-, or -(CH2)mY1(CH2)n-, wherein Y1 represents O, S, SO2, or CO and m and n each represent zero or 1 such that the sum of m+n is zero or 1; providing that when A represents a group of formula (a), any substituent present in Ar $i(ortho) to the carboxamide moiety is necessarily a hydrogen or a methoxy group; and salts thereof. Compounds of formula (I) and their salts have affinity for dopamine receptors, in particular the D3 receptor, and thus potential in the treatment of conditions wherein modulation of the D3 receptor is beneficial, e.g. as antipsychotic agents.
(FR) L'invention concerne des composés de la formule (I), dans laquelle R représente un substituant sélectionné parmi un hydrogène ou un substituant tel que défini dans les revendications. R2 représente un atome d'hydrogène ou un groupe alkyle C1-4; q est égal à 1 ou 2; A représente un groupe de la formule (a), (b) ou (c) où Ar représente une chaîne phényle éventuellement substituée ou une chaîne hétérocyclique aromatique à 5 ou 6 éléments, éventuellement substituées; ou une chaîne bicyclique éventuellement substituée; Ar1 et Ar2 représentent, chacun, indépendamment, une chaîne phényle éventuellement substituée ou une chaîne hétérocyclique aromatique à 5 ou 6 éléments, éventuellement substituée; et Y représente une liaison, -NHCO-, -CONH-, -CH2-, ou -(CH2)mY1(CH2)n-, où Y1 représente O, S, SO2 ou CO et m et n représentent chacun zéro ou 1 de telle sorte que la somme m+n est égale à zéro ou 1; à condition que A représente un groupe de la formule (a). Selon l'invention, tout substituant présent dans Ar en position ortho par rapport à la fraction de carboxamide est nécessairement un groupe hydrogène ou méthoxy; et l'invention concerne ausii des sels de ces derniers. Les composés de la formule (I) et leurs sels présentent une affinité pour les récepteurs de la dopamine, en particulier le récepteur D3, et ainsi offrent une utilité pour traiter les états dans lequels il est souhaitable de moduler le récepteur D3, par exemple, comme agents antipsychotiques.
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Designated States: AL, AM, AT, AU, AZ, BA, BB, BG, BR, BY, CA, CH, CN, CU, CZ, DE, DK, EE, ES, FI, GB, GE, GH, GM, GW, HU, ID, IL, IS, JP, KE, KG, KP, KR, KZ, LC, LK, LR, LS, LT, LU, LV, MD, MG, MK, MN, MW, MX, NO, NZ, PL, PT, RO, RU, SD, SE, SG, SI, SK, SL, TJ, TM, TR, TT, UA, UG, US, UZ, VN, YU, ZW
African Regional Intellectual Property Organization (ARIPO) (GH, GM, KE, LS, MW, SD, SZ, UG, ZW)
Eurasian Patent Office (AM, AZ, BY, KG, KZ, MD, RU, TJ, TM)
European Patent Office (EPO) (AT, BE, CH, CY, DE, DK, ES, FI, FR, GB, GR, IE, IT, LU, MC, NL, PT, SE)
African Intellectual Property Organization (BF, BJ, CF, CG, CI, CM, GA, GN, ML, MR, NE, SN, TD, TG)
Publication Language: English (EN)
Filing Language: English (EN)